Junior Validation Manager

Join Jamjoom Pharma as a Junior Validation Manager – Quality Department

Are you a detail-oriented professional with a passion for quality assurance in the pharmaceutical industry?

Jamjoom Pharma is looking for a dedicated Junior Validation Manager to strengthen our Quality team. In this role, you’ll play a vital part in ensuring product integrity, regulatory compliance, and operational excellence. Your expertise will help shape validation strategies that support smarter decisions, enhance performance, and drive sustainable growth across our manufacturing operations.

Key Responsibilities

• Prepare and execute Process Validation Protocols and Reports for new and existing products (Prospective, Concurrent, Retrospective).

• Develop and implement Cleaning Validation Protocols that meet global standards.

• Oversee all Process and Cleaning Validation activities, ensuring full compliance with cGMP and regulatory guidelines.

• Collect, review, and verify complete documentation for validation processes.

• Prepare Process Validation files for export markets, including CTD and eCTD formats.

• Lead Performance Qualification (PQ) for machines, utilities, and production equipment.

• Participate in Computerized System Validation (CSV) activities to support data integrity and system compliance.

• Collaborate cross-functionally with QA, Production, Engineering, and RA teams to drive validation strategy.

What We’re Looking For

• Proven experience in pharmaceutical validation.

• Strong knowledge of regulatory frameworks (ICH, WHO, FDA, EMA, GMP, and other international validation guidelines).

• Detail-oriented, organized, and proactive leadership style.

• Excellent documentation and communication skills.

Qualifications & Experience

• Bachelor’s degree in pharmacy (mandatory).

• Minimum of 10 years of hands-on experience in Validation and Qualification within the pharmaceutical industry.

• Proven experience in preparing CTD/eCTD dossiers for international markets.

• Practical knowledge in process validation, cleaning validation, equipment qualification (IQ/OQ/PQ), and CSV.

• Strong analytical and documentation skills.